Canonical Allele Identifier: PA2825601385
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376595
ClinVar Variation Id: 634778
ClinVar Variation Id: 1431729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Phe270Leu
CA16603017
NM_001126112.3:c.810T>G
CA397837037
NM_001126112.3:c.810T>A
CA397837052
NM_001126112.3:c.808T>C